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毒蕈碱受体激活导致细胞内钙升高,从而在稳定转染的细胞系中阻断电压激活的大鼠外向钾通道。

Elevation of intracellular calcium by muscarinic receptor activation induces a block of voltage-activated rat ether-à-go-go channels in a stably transfected cell line.

作者信息

Stansfeld C E, Röper J, Ludwig J, Weseloh R M, Marsh S J, Brown D A, Pongs O

机构信息

Zentrum für Moleculare Neurobiologie, Universität Hamburg, Germany.

出版信息

Proc Natl Acad Sci U S A. 1996 Sep 3;93(18):9910-4. doi: 10.1073/pnas.93.18.9910.

Abstract

We have studied the properties of r-eag voltage-activated potassium channels in a stably transfected human embryonic kidney cell line. It was found that r-eag channels are rapidly and reversibly inhibited by a rise in intracellular calcium from 30 to 300 nM. The inhibition does not appear to depend on the activity of calcium-dependent kinases and phosphatases. The effect of calcium on r-eag channel activity was studied in inside-out membrane patches. Calcium inhibited r-eag channel activity with a mean IC50 of 67 nM. Activation of muscarinic receptors, generating calcium oscillations in the transfected cells, induced a synchronous inhibition of r-eag mediated outward currents. This shows that calcium can mediate r-eag current inhibition following muscarinic receptor activation. The data indicate that r-eag channels are calcium-inhibitable voltage-activated potassium channels.

摘要

我们研究了稳定转染的人胚肾细胞系中r-eag电压门控钾通道的特性。发现细胞内钙浓度从30 nM升高到300 nM时,r-eag通道会迅速且可逆地受到抑制。这种抑制似乎不依赖于钙依赖性激酶和磷酸酶的活性。在内面向外的膜片上研究了钙对r-eag通道活性的影响。钙抑制r-eag通道活性,平均IC50为67 nM。毒蕈碱受体的激活在转染细胞中产生钙振荡,诱导r-eag介导的外向电流同步抑制。这表明钙可介导毒蕈碱受体激活后r-eag电流的抑制。数据表明r-eag通道是钙抑制性电压门控钾通道。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8926/38528/592a91ca7bd5/pnas01522-0623-a.jpg

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